Canonical Allele Identifier: CA3711979

Gene: HLA-B

Linked Data

• dbSNP Id: rs1131159
• ExAC: 6:31324892 G / A
• gnomAD v4: 6-31357115-G-A
• MyVariant Identifiers: chr6:g.31324892G>A (hg19) ; chr6:g.31357115G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357115G>A , CM000668.2:g.31357115G>A	GRCh38
NC_000006.11:g.31324892G>A , CM000668.1:g.31324892G>A	GRCh37
NC_000006.10:g.31432871G>A	NCBI36
NG_023187.1:g.5098C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1517C>T
ENST00000481849.6:n.1517C>T
ENST00000497377.6:n.1517C>T
ENST00000640094.2:c.44C>T	ENSP00000491275.2:p.Ala15Val
ENST00000696558.1:c.44C>T	ENSP00000512716.1:p.Ala15Val
ENST00000696559.1:c.44C>T	ENSP00000512717.1:p.Ala15Val
ENST00000696560.1:c.44C>T	ENSP00000512718.1:p.Ala15Val
ENST00000696561.1:c.44C>T	ENSP00000512719.1:p.Ala15Val
ENST00000696562.1:c.44C>T	ENSP00000512720.1:p.Ala15Val
ENST00000412585.7:c.44C>T MANE Select	ENSP00000399168.2:p.Ala15Val
ENST00000412585.6:c.44C>T	ENSP00000399168.2:p.Ala15Val
ENST00000434333.1:c.-52C>T	ENSP00000405931.1:n.-52C>T
ENST00000498007.1:n.65C>T
ENST00000603274.1:n.469G>A
NM_005514.6:c.44C>T	NP_005505.2:p.Ala15Val
XM_011514557.1:c.44C>T	XP_011512859.1:p.Ala15Val
XR_926175.1:n.54C>T
NM_005514.7:c.44C>T	NP_005505.2:p.Ala15Val
NM_005514.8:c.44C>T MANE Select	NP_005505.2:p.Ala15Val